@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP599958.RAZcvnA9EtJYQwZqXRtHzubpf8yCFoaiPpMW6to0JY9Ew130_head { this: np:hasAssertion dgn-np:NP599958.RAZcvnA9EtJYQwZqXRtHzubpf8yCFoaiPpMW6to0JY9Ew130_assertion; np:hasProvenance dgn-np:NP599958.RAZcvnA9EtJYQwZqXRtHzubpf8yCFoaiPpMW6to0JY9Ew130_provenance; np:hasPublicationInfo dgn-np:NP599958.RAZcvnA9EtJYQwZqXRtHzubpf8yCFoaiPpMW6to0JY9Ew130_publicationInfo; a np:Nanopublication . dgn-np:NP599958.RAZcvnA9EtJYQwZqXRtHzubpf8yCFoaiPpMW6to0JY9Ew130_assertion a np:Assertion . dgn-np:NP599958.RAZcvnA9EtJYQwZqXRtHzubpf8yCFoaiPpMW6to0JY9Ew130_provenance a np:Provenance . dgn-np:NP599958.RAZcvnA9EtJYQwZqXRtHzubpf8yCFoaiPpMW6to0JY9Ew130_publicationInfo a np:PublicationInfo . } dgn-np:NP599958.RAZcvnA9EtJYQwZqXRtHzubpf8yCFoaiPpMW6to0JY9Ew130_assertion { miriam-gene:4914 a ncit:C16612 . lld:C0238462 a ncit:C7057 . dgn-gda:DGN5eaebf2db3ef53df9cad0172f3edf59e sio:SIO_000628 miriam-gene:4914, lld:C0238462; a sio:SIO_001121 . } dgn-np:NP599958.RAZcvnA9EtJYQwZqXRtHzubpf8yCFoaiPpMW6to0JY9Ew130_provenance { dgn-np:NP599958.RAZcvnA9EtJYQwZqXRtHzubpf8yCFoaiPpMW6to0JY9Ew130_assertion dcterms:description "[Using a proteomic-multiplexed analysis of the phosphotyrosine signaling together with antibody-based validation techniques, we identified several candidate molecules for RET (rearranged during transfection) tyrosine kinase receptor carrying mutations responsible for the multiple endocrine neoplasia type 2A and 2B (MEN2A and MEN2B) syndromes in two human medullary thyroid carcinoma (MTC) cell lines, TT and MZ-CRC-1, which express the RET-MEN2A and RET-MEN2B oncoproteins, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:18756447; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP599958.RAZcvnA9EtJYQwZqXRtHzubpf8yCFoaiPpMW6to0JY9Ew130_publicationInfo { this: dcterms:created "2015-08-25T14:43:38+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }